STK11 c.862+145C>G

Variant ID: 19-1221484-C-G

NM_000455.4(STK11):c.862+145C>G

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs741764
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Unique Features of Germline Variation in Five Egyptian Familial Breast Cancer Families Revealed by Exome Sequencing.

Plos One
Kim, Yeong C YC; Soliman, Amr S AS; Cui, Jian J; Ramadan, Mohamed M; Hablas, Ahmed A; Abouelhoda, Mohamed M; Hussien, Nehal N; Ahmed, Ola O; Zekri, Abdel-Rahman Nabawy AN; Seifeldin, Ibrahim A IA; Wang, San Ming SM
Publication Date: 2017

Variant appearance in text: rs741764
PubMed Link: 28076423
Variant Present in the following documents:
  • pone.0167581.s001.xlsx, sheet 1
View BVdb publication page



Polymorphisms in immune function genes and non-Hodgkin lymphoma survival.

Journal Of Cancer Survivorship : Research And Practice
Aschebrook-Kilfoy, Briseis B; Zheng, Tongzhang T; Foss, Francine F; Ma, Shuangge S; Han, Xuesong X; Lan, Qing Q; Holford, Theodore T; Chen, Yingtai Y; Leaderer, Brian B; Rothman, Nathaniel N; Zhang, Yawei Y
Publication Date: 2012-03

Variant appearance in text: rs741764
PubMed Link: 22113576
Variant Present in the following documents:
  • Main text
View BVdb publication page



LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome.

Journal Of Medical Genetics
Volikos, E E; Robinson, J J; Aittomäki, K K; Mecklin, J-P JP; Järvinen, H H; Westerman, A M AM; de Rooji, F W M FW; Vogel, T T; Moeslein, G G; Launonen, V V; Tomlinson, I P M IP; Silver, A R J AR; Aaltonen, L A LA
Publication Date: 2006-05

Variant appearance in text: rs741764
PubMed Link: 16648371
Variant Present in the following documents:
  • Main text
View BVdb publication page